Status and phase
Conditions
Treatments
Study type
Funder types
Identifiers
About
The main purpose of this investigational research study is to determine how safe and tolerable the study drug siltuximab is in patients with myelofibrosis (MF). This medication has been approved by the FDA for another condition (multicentric castleman's disease (MCD), but not for myelofibrosis (MF). In MCD, siltuximab resulted in improvement in symptoms and anemia. While MCD and MF are different diseases, they share some common features including a protein call interleukin-6 (IL-6) that may be important in causing symptoms of MCD and MF.
Full description
PRIMARY OBJECTIVES:
I. To evaluate safety and tolerability of the drug siltuximab in the myelofibrosis patient population.
SECONDARY OBJECTIVES:
I. To determine clinical improvement (CI). II. To determine the overall response rate (ORR).
TERTIARY OBJECTIVES:
I. To determine if siltuximab results in improvement in iron dysregulation. II. To determine changes in inflammatory stress that may correlate with clinical response.
OUTLINE:
Patients receive siltuximab intravenously (IV) over 60 minutes on day 1. Patients also undergo bone marrow biopsy and aspiration at baseline and at the end of treatment (within 30 days of last siltuximab dose) or as clinically indicated. Treatment repeats every 21 days for up to 6 courses in the absence of disease progression, unacceptable toxicity, or patient decision to withdraw. Patients who are responding after 6 courses may receive additional siltuximab treatment for up to 1 year at the discretion of the study doctor.
After completion of study treatment, patients are followed up at 30 days.
Sex
Ages
Volunteers
Inclusion criteria
Patients must have a histologically confirmed diagnosis of primary myelofibrosis (PMF), post-polycythemia vera (post-PV) myelofibrosis (MF), or post-essential thrombocythemia (post-ET) MF using World Health Organization Criteria
Patients must have disease that requires therapy, including intermediate-1, intermediate-2, or high-risk disease according to the International Prognostic Scoring System (IPSS) or Dynamic-IPSS
Patients must be off myeloproliferative neoplasm (MPN) directed therapy, such as Janus kinase (JAK)-inhibitors, for at least 2 weeks prior to administration of the study drug; NOTE: This does not include supportive transfusion, or hydroxyurea; these must be stopped prior to first day of treatment, but no wash -out period is required
Patients must be resistant to, intolerant of, or ineligible for JAK2 inhibitor therapy, based on severe anemia or thrombocytopenia
Patients must exhibit an Eastern Cooperative Oncology Group (ECOG) performance status of =< 2
New York Heart Association functional classification for congestive heart failure (NYHA CHF) < 3
Patients must have clinical laboratory values meeting the following criteria within 28 days prior to registration:
Absolute neutrophil count >= 1.0 x 10^9/L (without growth factor support)
Platelet count >= 20 x 10^9/L (without transfusion support within 2 weeks of registration)
Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =< 2.5 x upper limit of normal (ULN)
Alkaline phosphatase =< 2.5 x ULN
Total bilirubin =< 2.5 x upper limit of normal (ULN) except if the elevation is due to Gilbert's syndrome (allowable at =< 5 x ULN) or myelofibrosis (per principle investigator [PI] discretion)
Calculated creatinine clearance > 20 mL/min per institutional standard
Before enrollment, a woman must be one of the following:
Not of childbearing potential, defined as:
Of childbearing potential and practicing a highly effective method of birth control (consistent with local regulations regarding the use of birth control methods for subjects participating in clinical studies) during the study and for 3 months after receiving the last dose of study agent NOTE: Examples include established use of oral, injected or implanted hormonal methods of contraception; placement of an intrauterine device (IUD) or intrauterine system (IUS); barrier methods: condom with spermicidals (including foam/gel/film/cream/suppository) or occlusive cap (diaphragm or cervical/vault caps) with spermicidals; male partner sterilization (the vasectomized partner should be the sole partner for that subject); true abstinence (when this is in line with the preferred and usual lifestyle of the subject); Note: If the childbearing potential changes after start of the study (e.g., woman who is not heterosexually active becomes active) a woman must begin a highly effective method of birth control, as described above
Women of childbearing potential must have a negative urine or serum pregnancy test within 7 days prior to registration
Female patients must agree (during the study and for 3 months after receiving the last dose of study agent, not to donate eggs (ova, oocytes) for the purposes of assisted reproduction
A man who is sexually active with a woman of childbearing potential and has not had a vasectomy must agree to use a barrier method of birth control e.g., either condom with spermicidals or partner with occlusive cap with spermicidals and all men must also not donate sperm during the study and for 3 months after receiving the last dose of study drug
Patients must have the ability to understand and the willingness to sign a written informed consent prior to registration on study
Patients must be willing and able to adhere to the prohibitions and restrictions specified in this protocol
Exclusion criteria
Patients with prior exposure to agents targeting interleukin 6 (IL -6) or the IL-6 receptor are not eligible
Patients with another malignancy, unless they have been disease free for 2 years prior to registration, with the exception of
Patients who have an uncontrolled intercurrent illness including, but not limited to any of the following, are not eligible:
Patients who have received vaccination with live attenuated vaccines within 6 months prior to registration are not eligible
Patients who are on any prohibited medication; they have to be have a wash-out period of at least 2 weeks prior to registration, in order to be eligible for the study
Patients with clinically significant infection, including known human immunodeficiency virus (HIV), human herpesvirus-8 (HHV-8), hepatitis C infection, or known hepatitis B surface antigen positivity are not eligible
Female patients who are pregnant or breast-feeding are not eligible; NOTE: A woman who is planning to become pregnant or a man who plans to father a child while enrolled in this study or within 3 months after the last dose of study agent should likewise not be considered for this study
Patients who have received an investigational drug (including investigational vaccines) or used an invasive investigational medical device within 14 days or 5 half -lives before registration or is currently enrolled in the treatment stage of an investigational study are not eligible; please contact PI for further details on wash-out period and eligibility of such patients
Patients who have been hospitalized for infection or major surgery (e.g., requiring general anesthesia) within 2 weeks before registration or have not fully recovered from surgery are not eligible; Note: Subjects with surgical procedures conducted under local anesthesia may participate
Patients who are unwilling or unable to comply with the protocol
Primary purpose
Allocation
Interventional model
Masking
0 participants in 1 patient group
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal